Philip M. Parker's Carnitine Palmitoyltransferase I Deficiency - A Bibliography PDF

By Philip M. Parker

ISBN-10: 0071459960

ISBN-13: 9780071459969

ISBN-10: 0497113465

ISBN-13: 9780497113469

In March 2001, the nationwide Institutes of well-being issued the next caution: "The variety of websites supplying health-related assets grows on a daily basis. Many websites supply priceless details, whereas others could have details that's unreliable or misleading." additionally, a result of fast bring up in Internet-based info, many hours could be wasted looking, choosing, and printing. considering that merely the smallest fraction of knowledge facing Carnitine palmitoyltransferase I deficiency is listed in se's, reminiscent of or others, a non-systematic method of web learn will be not just time eating, but additionally incomplete. This publication was once created for doctors, scholars, and individuals of most of the people who are looking to behavior clinical study utilizing the main complex instruments to be had and spending the smallest amount of time doing so.

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Additional resources for Carnitine Palmitoyltransferase I Deficiency - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers

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Conditions caused by many contributing factors are called complex or multifactorial disorders. Although complex disorders often cluster in families, they do not have a clear-cut pattern of inheritance. This makes it difficult to determine a person’s risk of inheriting or passing on these disorders. Complex disorders are also difficult to study and treat because the specific factors that cause most of these disorders have not yet been identified. By 2010, however, researchers predict they will have found the major contributing genes for many common complex disorders.

A repeat expansion is a mutation that increases the number of times that the short DNA sequence is repeated. This type of mutation can cause the resulting protein to function improperly. Can Changes in Chromosomes Affect Health and Development? Changes that affect entire chromosomes or segments of chromosomes can cause problems with growth, development, and function of the body’s systems. These changes can affect many genes along the chromosome and alter the proteins made by those genes. Conditions caused by a change in the number or structure of chromosomes are known as chromosomal disorders.

These factors usually affect disorders that have an autosomal dominant pattern of inheritance, although they are occasionally seen in disorders with an autosomal recessive inheritance pattern. Reduced Penetrance Penetrance refers to the proportion of people with a particular genetic change (such as a mutation in a specific gene) who exhibit signs and symptoms of a genetic disorder. If some people with the mutation do not develop features of the disorder, the condition is said to have reduced (or incomplete) penetrance.

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Carnitine Palmitoyltransferase I Deficiency - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers by Philip M. Parker

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